Canonical Allele Identifier: CA89521476

Gene: EHHADH

Linked Data

• dbSNP Id: rs1019622299
• gnomAD v4: 3-185253931-G-A
• MyVariant Identifiers: chr3:g.184971719G>A (hg19) ; chr3:g.185253931G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185253931G>A , CM000665.2:g.185253931G>A	GRCh38
NC_000003.11:g.184971719G>A , CM000665.1:g.184971719G>A	GRCh37
NC_000003.10:g.186454413G>A	NCBI36
NG_015999.1:g.5168C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.74+18C>T MANE Select	ENSP00000231887.3:n.74+18C>T
ENST00000231887.7:c.74+18C>T	ENSP00000231887.3:n.74+18C>T
ENST00000440662.1:c.74+18C>T	ENSP00000396798.1:n.74+18C>T
ENST00000456310.5:c.-320C>T	ENSP00000387746.1:n.-320C>T
ENST00000465178.1:n.228-5414C>T
ENST00000475987.1:n.101+18C>T
NM_001166415.1:c.-320C>T	NP_001159887.1:n.-320C>T
NM_001966.3:c.74+18C>T	NP_001957.2:n.74+18C>T
XM_006713525.1:c.-582+18C>T	XP_006713588.1:n.-582+18C>T
XM_011512517.1:c.-214-5414C>T	XP_011510819.1:n.-214-5414C>T
NM_001966.4:c.74+18C>T MANE Select	NP_001957.2:n.74+18C>T
NM_001166415.2:c.-320C>T	NP_001159887.1:n.-320C>T